DNAJB11 Mutation in ADPKD Patients: Clinical Characteristics in a Monocentric Cohort

Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a late-onset cilia-related disorder, characterized by progressive cystic enlargement of the kidneys. It is genetically heterogeneous with PKD1 and PKD2 pathogenic variants identified in approximately 78% and 15% of families, respectively. More recently, additional ADPKD genes, such as DNAJB11, have been identified and included in the diagnostic routine test for renal cystic diseases. However, despite recent progress in ADPKD molecular approach, approximately ~7% of ADPKD-affected families remain genetically unresolved. We collected a cohort of 4 families from our center, harboring heterozygous variants in the DNAJB11 gene along with clinical and imaging findings consistent with previously reported features in DNAJB11 mutated patients. Mutations were identified as likely pathogenetic (LP) in three families and as variants of uncertain significance (VUS) in the remaining one. One patient underwent to kidney biopsy and showed a prevalence of interstitial fibrosis that could be observed in ~60% of the sample. The presence in the four families from our cohort of ADPKD characteristics together with ADTKD features, such as hyperuricemia, diabetes, and chronic interstitial fibrosis, supports the definition of DNAJB11 phenotype as an overlap disease between these two entities, as originally suggested by the literature.


Introduction
Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a late-onset cilia-related disorder, characterized by progressive cystic enlargement of the kidneys [1,2].ADPKD can be defined as a multisystemic condition, as it presents both renal and extra-renal manifestations.The kidneys are involved with cystic bilateral enlargement, which causes other renal-related consequences such as hypertension and urological events.
ADPKD is the fourth leading cause of end-stage renal disease (ESRD) worldwide and the most common form of monogenic cystic kidney disease as it leads to kidney failure in more than 50% of patients by the age of 60.It is also the most common of all the inherited cases of chronic kidney disease (CKD) [2].
This disorder is genetically heterogeneous with PKD1 and PKD2 pathogenic variants identified in approximately 78% and 15% of families, respectively [3].More recently additional ADPKD causative genes have been identified and included in diagnostic routine tests for renal cystic diseases.However, approximately ~7% of ADPKD-affected families remain genetically unresolved [4].
In 2018, Cornec-Le Gall et al. [4] first described monoallelic pathogenic variants in DNAJB11 as a cause of cystic kidney disease, accounting for ~1.2% of ADPKD or ADPLD unresolved affected families.The clinical phenotype of patients harboring mutations in this gene was characterized by non-enlarged cystic kidneys that often evolved to kidney atrophy, while ESRD was reached later than typical genetic cases of ADPKD, from 59 to 89 years.
To date, due to the rarity of DNAJB11 involvement in kidney diseases, limited reports are available in the literature.We present a case series of four families harboring monoallelic DNAJB11 variants, with clinical and histological characteristics.
The selection criteria were the presence of a mutation in DNAJB11, the absence of mutations in PKD1/PKD2, the presence of bilateral millimetric cysts in the kidneys, and an age > 18 years.Before performing the genetic test, patients had signed an informed consent.Ethical review and approval were waived for this study because, according to the local policy, informed consent is considered sufficient for reports of an observational nature concerning a limited number of patients.
Clinical, imaging, and histological data were obtained by review of clinical records.Arterial hypertension was considered as blood pressure ≥140/90 mmHg or positive history of antihypertensive therapy, eGFR was calculated from the serum creatinine measurement using the CKD-EPI equation and expressed as mL/min/1.73m 2 .Extra-renal involvement was evaluated by consulting clinical records, considering T2DM, renal colics, hypertension, hyperuricemia, presence of family members with ESRD, and pathological findings at the echocardiogram, as well as the presence of family members with aneurysms, or related symptoms.
The possible presence of a kidney biopsy was also assessed.When present, the routine histological staining procedures were performed on 3-µm-thick sections, including immunofluorescence (IF) studies and electron microscopy.IF was conducted on frozen sections and stained with antisera for IgG, IgA, IgM, C3, kappa, and lambda chains.
In addition, we compared data related to our cohort with the ones described by previous literature published articles.

Study Participants and Clinical Analysis
We selected a cohort of 5 patients, belonging to 4 families and with a 5-years follow-up.

Family 1
A 67-year-old male (Patient 1), during a follow-up for a Monoclonal Gammopathy of Undetermined Significance (MGUS) IIgG/k discovered previously, was found on September 2019 with a creatinine of 1.58 mg/dL and an eGFR of 46 mL/min/1.73m 2 .The abdominal US and MRI showed the presence of regular-sized kidneys (both were 10 cm) with cortical millimetric cysts, while no cysts were detected in the liver (see Figure 1).The possible presence of a kidney biopsy was also assessed.When present, the routine histological staining procedures were performed on 3-μm-thick sections, including immunofluorescence (IF) studies and electron microscopy.IF was conducted on frozen sections and stained with antisera for IgG, IgA, IgM, C3, kappa, and lambda chains.
In addition, we compared data related to our cohort with the ones described by previous literature published articles.

Study Participants and Clinical Analysis
We selected a cohort of 5 patients, belonging to 4 families and with a 5-years followup.

Family 1
A 67-year-old male (Patient 1), during a follow-up for a Monoclonal Gammopathy of Undetermined Significance (MGUS) IIgG/k discovered previously, was found on September 2019 with a creatinine of 1.58 mg/dL and an eGFR of 46 mL/min/1.73m 2 .The abdominal US and MRI showed the presence of regular-sized kidneys (both were 10 cm) with cortical millimetric cysts, while no cysts were detected in the liver (see Figure 1).A kidney biopsy was performed and analyzed with light microscopy, immunofluorescence, and electronic microscopy (see Figure 2).Multiple sections of light microscopy were prepared.The biopsy consisted of 1 piece of cortex containing up to 9 glomeruli, 7 of which were globally sclerosed, some of which are in a solidified pattern.No hypercellularity was found in the remaining glomeruli.There was a patchy disproportionate interstitial fibrosis with less tubular atrophy in around 60% of the sample and few tubular cysts.In addition, there were features consistent with moderate to severe arterionephrosclerosis, with moderate to severe thickening of tunica media and moderate intima fibrosis of interlobular arteries and arterioles.Immunofluorescence was negative for immunocomplex mediate, and immunomediate, as well as monoclonal component.Electron microscopy confirmed the features found in light microscopy and IF studies.A kidney biopsy was performed and analyzed with light microscopy, immunofluorescence, and electronic microscopy (see Figure 2).Multiple sections of light microscopy were prepared.The biopsy consisted of 1 piece of cortex containing up to 9 glomeruli, 7 of which were globally sclerosed, some of which are in a solidified pattern.No hypercellularity was found in the remaining glomeruli.There was a patchy disproportionate interstitial fibrosis with less tubular atrophy in around 60% of the sample and few tubular cysts.In addition, there were features consistent with moderate to severe arterionephrosclerosis, with moderate to severe thickening of tunica media and moderate intima fibrosis of interlobular arteries and arterioles.Immunofluorescence was negative for immunocomplex mediate, and immunomediate, as well as monoclonal component.Electron microscopy confirmed the features found in light microscopy and IF studies.
The subject manifested hypertension at 67 years.He presented a tendency to progressive CKD with a loss of eGFR of −4 mL/min/1.73m 2 /year, and a serum creatinine, at the last follow-up, of 2.50 mg/dL with an eGFR of 26 mL/min/1.73m 2 .Due to the presence of kidney cysts, he was also evaluated for extra-renal manifestations: the liver did not present any cysts, the heart was not affected by any valvulopathy, and the MRI of the brain did not show any aneurysm (only a frontal angioma was present).The patient also presented hyperuricemia.Due to the presence of an atypical cystic phenotype, genetic testing was performed to identify mutations in genes related to Autosomal Dominant Polycystic Kidney Disease (ADPKD) and other cystic nephropathies.NGS analysis showed likely pathogenic (LP) heterozygous novel variant c.716 T>G (p.Leu239Ter) in DNAJB11; it was absent from the population database (gnomAD), CADD 40.The subject manifested hypertension at 67 years.He presented a tendency to progressive CKD with a loss of eGFR of −4 mL/min/1.73m 2 /year, and a serum creatinine, at the last follow-up, of 2.50 mg/dL with an eGFR of 26 mL/min/1.73m 2 .Due to the presence of kidney cysts, he was also evaluated for extra-renal manifestations: the liver did not present any cysts, the heart was not affected by any valvulopathy, and the MRI of the brain did not show any aneurysm (only a frontal angioma was present).The patient also presented hyperuricemia.Due to the presence of an atypical cystic phenotype, genetic testing was performed to identify mutations in genes related to Autosomal Dominant Polycystic Kidney Disease (ADPKD) and other cystic nephropathies.NGS analysis showed likely pathogenic (LP) heterozygous novel variant c.716 T>G (p.Leu239Ter) in DNAJB11; it was absent from the population database (gnomAD), CADD 40.
As for the family history (see Figure 3), his mother died at the age of 86 years, presenting a mild chronic kidney disease in her last decade of life.The proband has four brothers: one died at the age of 69 from a cerebral tumor (II-2), and another one, brother II-5, was not available for testing.The other two brothers were evaluated for the presence of the mutation: subject II-3, age 72, affected by Type 2 Diabetes Mellitus, tested positive for the familial DNAJB11 variant and his laboratory test demonstrated a reduction of eGFR (59 mL/min/1.73m 2 ) and a slight increase in serum creatinine (1.23 mg/dL), without proteinuria (UACr < 5 mg/g).No kidney or liver cysts were detected by abdominal ultrasound.The youngest brother (II-4), age 61, did not harbor the familial DNAJB11 variant, and his eGFR and serum creatinine were normal (87 mL/min/1.73m 2 and 0.94 mg/dL).Despite the lack of ultrasound renal anomalies in subject II-3, proband's phenotype and chronic kidney disease in his family support the causative role of the variant.As for the family history (see Figure 3), his mother died at the age of 86 years, presenting a mild chronic kidney disease in her last decade of life.The proband has four brothers: one died at the age of 69 from a cerebral tumor (II-2), and another one, brother II-5, was not available for testing.The other two brothers were evaluated for the presence of the mutation: subject II-3, age 72, affected by Type 2 Diabetes Mellitus, tested positive for the familial DNAJB11 variant and his laboratory test demonstrated a reduction of eGFR (59 mL/min/1.73m 2 ) and a slight increase in serum creatinine (1.23 mg/dL), without proteinuria (UACr < 5 mg/g).No kidney or liver cysts were detected by abdominal ultrasound.The youngest brother (II-4), age 61, did not harbor the familial DNAJB11 variant, and his eGFR and serum creatinine were normal (87 mL/min/1.73m 2 and 0.94 mg/dL).Despite the lack of ultrasound renal anomalies in subject II-3, proband's phenotype and chronic kidney disease in his family support the causative role of the variant.

Family 2
A 67-years-old male (Patient 2) came under observation for the occurrence of nephrolithiasis.An abdominal US looking for the kidney stones highlighted the presence of regularsized kidneys (right kidney was 11 cm, left kidney was 13 cm) with bilateral millimetric cysts.The patient later underwent an abdominal MRI (see Figure 1) that confirmed the ultrasound findings, also describing some cysts of increased dimensions (the biggest one in the right kidney with a diameter of 26 mm) while no cysts were identified in the liver.The patient also suffered from an acute myocardial infarction at 55 years, atrial fibrillation at 62 years, and hypertension.During the clinical assessment for extra-renal manifestations, an echocardiogram was performed showing the presence of a severe mitral insufficiency.He presented a tendency to progressive CKD with a loss of eGFR of −4.3 mL/min/1.73m 2 /year.The serum creatinine at the last follow-up was 4.16 mg/dL and the eGFR was 14 mL/min/1.73m 2 , while his uric acid was 9.3 mg/dL.NGS analysis for ADPKD and other cystic nephropathy genes identified a heterozygous likely pathogenic variant in DNAJB11 (c.134A>G, p.Tyr45Cys), CADD 27.3.

Family 2
A 67-years-old male (Patient 2) came under observation for the occurrence of nephrolithiasis.An abdominal US looking for the kidney stones highlighted the presence of regular-sized kidneys (right kidney was 11 cm, left kidney was 13 cm) with bilateral millimetric cysts.The patient later underwent an abdominal MRI (see Figure 1) that confirmed the ultrasound findings, also describing some cysts of increased dimensions (the biggest one in the right kidney with a diameter of 26 mm) while no cysts were identified in the liver.The patient also suffered from an acute myocardial infarction at 55 years, atrial fibrillation at 62 years, and hypertension.During the clinical assessment for extra-renal manifestations, an echocardiogram was performed showing the presence of a severe mitral insufficiency.He presented a tendency to progressive CKD with a loss of eGFR of −4.3 mL/min/1.73m 2 /year.The serum creatinine at the last follow-up was 4.16 mg/dL and the eGFR was 14 mL/min/1.73m 2 , while his uric acid was 9.3 mg/dL.NGS analysis for ADPKD and other cystic nephropathy genes identified a heterozygous likely pathogenic variant in DNAJB11 (c.134A>G, p.Tyr45Cys), CADD 27.3.
As for family history (see Figure 3), his mother died at 83 years and suffered from nephrolithiasis throughout her life.All his three sisters are not known to be interested in any renal disease.Only one of them was reported to be affected by recurrent cholelithiasis.No sister was available for the segregation analysis.As for family history (see Figure 3), his mother died at 83 years and suffered from nephrolithiasis throughout her life.All his three sisters are not known to be interested in any renal disease.Only one of them was reported to be affected by recurrent cholelithiasis.No sister was available for the segregation analysis.

Family 3
A 61-years-old female (Patient 3), with a positive family history of cystic nephropathies, underwent an abdominal ultrasound during the follow-up, which found regular-sized kidneys (right kidney was 10.9, left kidney was 10.5 cm) with bilateral millimetric cysts, some of which were calcified.The liver was not involved in any cyst.A CT confirmed the absence of enlarged kidneys and liver cysts (see Figure 1).The patient presented microhematuria since the age of 47 years old and hypertension since the age of 55 years old, in addition, she suffered from recurrent cystitis and had a renal colic at 60 years old.As part of the ongoing follow-up, a mild tricuspid insufficiency was discovered by an echocardiogram in 2012, as well as a mild neurosensorial hearing loss in the left ear.
She presented a tendency to progressive CKD with a loss of eGFR of −2.3 mL/min/ 1.73 m 2 /year.The creatinine at the last follow-up was 1.14 mg/dL and the eGFR of 52 mL/min/1.73m 2 .Due to the discovery of cysts in the kidneys, the patient was investigated for mutations in genes related to cystic nephropathies, and a heterozygous likely pathogenic variant in DNAJB11 was found (c.456+3_456+6del).
As for the family history (see Figure 3), the subject's mother presented with multicystic kidneys and died after being on hemodialysis for nine years.The maternal grandmother of the subject was probably affected by a kidney disease as well, as she underwent a nephrectomy for unknown causes.The brother underwent an ultrasound showing microlithiasis, while his renal function showed a creatinine of 0.88 mg/dL and an eGFR of 90 mL/min/1.73m 2 .The genetic testing was negative for the family mutation.
A 59-years-old female (Patient 4) was also assessed.She is a maternal cousin of Patient 3 (see Figure 3).Her mother passed away at 39 years old due to an asthma crisis, as a result of this the presence of kidney disease could not be established.Patient 4 underwent an abdominal ultrasound that showed the presence of cysts in the kidneys and the liver: the kidneys had a normal size (right one of 10.3 cm and left one of 9.4 cm) and presented bilateral millimetric cysts, some of which were calcified.A CT was also performed confirming the ultrasound discoveries (see Figure 3).
She has suffered from hypertension since she was 50 years old.Her serum creatinine at the time of the evaluation was 1.27 mg/dL and her eGFR was 46 mL/min/1.73m 2 .She was tested for the DNAJB11 variant found in her cousin (c.456+3_456+6del), with a positive result.

Family 4
A 46-years-old female (Patient 5) came under observation because she developed hypokalaemia and long QT, probably as a result of the anti-depressant drugs that she was on, and was, consequently, hospitalized at our center.Before being admitted to the hospital, indeed, she stayed in a psychiatric facility for a reactive anxiety depressive syndrome for which she was being treated.During her hospitalization her kidneys were assessed with a CT and an MRI, both showing the presence of regular-sized kidneys (both were 10 cm) with bilateral millimetric cysts (the biggest one of 33 mm) (see Figure 3).The liver presented just one cyst in the III segment with a diameter of 4 mm.The serum creatinine was 1.54 mg/dL and the eGFR was 40 mL/min/1.73m 2 , and she also presented hyperuricemia.Genetic testing for cystic nephropathies was performed and found a heterozygous c.499C>T (p.Arg167Trp) variant, classified as a variant of unknown significance; CADD 31.Her family history (see Figure 1) showed the presence of renal disease in the father, who was not available for an assessment.The patient did not carry on a follow-up, so longitudinal data are not available.
A summary of the main clinical, imaging, and laboratory characteristics of all patients can be found in Table 1.A specific section was dedicated to the extra-renal involvement, highlighting how DNAJB11-ADPKD can be described as a multisystemic syndrome.

Discussion
ADPKD is an inherited multisystemic condition characterized by the presence of cysts in the kidneys, often in the liver, and many other sites.It is associated with an increased kidney volume, due to the cysts' growth.The Pei's criteria, [6] based on the number of cysts for each kidney and the patient's age, allow the clinical diagnosis.The Mayo Clinic Imaging Classification created two classes according to the imaging criteria [7] differentiating typical and atypical forms.Class 1 represents a typical imaging pattern, defined by bilateral and diffuse cyst distribution causing nephromegaly.By contrast, class 2 is characterized by a unilateral, asymmetric, segmental, lopsided, or bilateral cystic distribution with unilateral or bilateral kidney atrophy.Typical and atypical imaging are directly related to the genotype [8].Indeed, PKD1 and PKD2 are the two more frequent mutated genes and are linked to a typical aspect at the CT and MRI scans.On the other hand, genes described as "atypical", such as GANAB, PKHD1, DZIP1L, ALG8, and SEC61A1, are associated with Class 2 according to the Mayo Classification.
Pathogenic variants in the DNAJB11 gene have been recently discovered as a cause of cystic kidney disease.The clinical phenotype related to this condition has been described in previous articles, but, being this a rare mutation, there is still a need for case reports that permit to better description of clinical aspects in patients harboring the mutation.DNAJB11 (located on chromosome 3q27.3)encodes a 358-amino acid soluble glycoprotein called ERdj3, which functions as a binding immunoglobulin protein (BiP) co-chaperone, playing a central role in the maintenance of the endoplasmic reticulum (ER) protein homeostasis [9].BiP (also known as GRP78) is, indeed, a heat shock protein chaperone required for the proper folding and assembly of proteins in the ER.It targets misfolded proteins to ER degradation and acts as a master regulator of the unfolded protein response, an adaptive cellular response to ER stress [10].DNAJB11-protein interacts with BiP through a highly conserved J domain, with a characteristic His-Pro-Asp (HPD) motif [10].The altered mechanism in protein folding is the cause of a loss of maturation and appropriate localization of polycystin-1, the protein encoded by PKD1, resulting in renal and liver cystogenesis [3,4,11].Polycystin-1 is particularly susceptible to dosage reduction of proteins involved in maturation and trafficking in the ER, leading to a loss of function, which was described as the main mechanism of initiation and enlargement of kidney and liver cysts [3,[11][12][13].
The literature, as for the phenotype of patients with DNAJB11 mutations, described non-enlarged cystic kidneys, together with ESRD reached later in life than typical ADPKD.In addition to these features, interstitial fibrosis, evident in non-cystic parenchyma, as well as recurring episodes of gout and hyperuricemia could also be found in these patients.The liver, unlike in typical ADPKD, has been reported to be less involved [4].These elements indicate that DNAJB11 is the responsible mutated gene for an atypical dominant form of ADPKD [4].
Four variants were detected in our cohort, three of which were defined as likely pathogenic and the other one as a variant of uncertain significance.Patients did not show mutations in any gene analyzed in the cystic nephropathies' panel, apart from DNAJB11.To better classify the role of the variant described in Family 1, we carried out a segregation familial analysis: the proband's brother, who tested positive for the familial variant, did not show any cyst at the ultrasound even if his serum creatinine was increased.However, a second level of imaging has not been performed yet, and this could be decisive in the discovery of millimetric kidney cysts, not detectable at the ultrasound.The kidney biopsy performed on Patient 1 was another important tool to better define the disease.It showed a disproportionate presence between interstitial fibrosis and tubular atrophy, with a prevalence of interstitial fibrosis that could be observed in ~60% of the sample.Moreover, the presence of macrophages was another important discovery, as their presence can be related to the continuous production of fibrotic material with a neverending mechanism.A kidney biopsy, performed in a previous study on a patient with a mutation in DNAJB11, similarly showed the presence of tubular cysts and moderate arteriosclerosis, but much less interstitial fibrosis [14].Therefore, the result from the biopsy later than typical ADPKD patients.In the patients from Bologna, a mean value of eGFR of 35.6 ± 15.5 mL/min/1.73m 2 was observed with a mean loss of eGFR per year of −3.5 ± 1.1 mL/min/1.73m 2 .Three out of the five probands that were evaluated in the present study had a follow-up > 4 years, showing a typical ADPKD rapid progressor behavior with an eGFR loss > 3 mL/min/1.73m 2 /year, according to the ErkNet Position Statement of 2022 [17].However, in consideration of the normal TKV and the absence of liver cysts, the Bologna cohort could be considered analogous to the atypical form of ADPKD.
Finally, we compared the presence of associated conditions among patients belonging to the different cohorts.Nephrolithiasis, hyperuricemia, and cardiovascular defects were the features most present in all cohorts.
A pathogenic variant in DNAJB11 was observed in the literature to be associated with the retention of uromodulin in the cytoplasm caused by an altered mechanism in folding and cellular trafficking of proteins, also related to a mutation in UMOD [4,14].This mechanism could be associated with the recurrence of hyperuricemia and Type 2 Diabetes Mellitus in these patients.Pisani et al. [15], in addition, showed how this feature could be found only in patients with the DNAJB11 mutation, while not in patients with ADPKD.An in vivo study [18], on the contrary, demonstrated the absence of change in uromodulin processing in Dnajb11 knock-out mice, while showing an impaired cleavage of polycystin-1 dosage-dependent cystogenesis.Another in vitro study [19], consistent with the latter, demonstrated that the excretion, maturation, and trafficking of uromodulin are unchanged in patients with DNAJB11 mutations.Further functional studies are needed to better define the pathophysiology behind the disease caused by a mutation in DNAJB11.
In conclusion, DNAJB11 mutation, according to the findings in patients from the literature and our cohort, is related to a specific cystic disease phenotype.Moreover, the association between hyperuricemia, diabetes, and the eGFR time-dependent decrease, together with the presence of chronic interstitial fibrosis at the biopsy and of small renal cysts, indicates that this condition is characterized by partial phenotypic overlap between ADPKD and autosomal dominant tubulointerstitial diseases (ADTKD) [4].Furthermore, the prevalence of characteristics defining an atypical disease must be highlighted.The small number of patients analyzed by the literature and implemented by our cohort, and the follow-up data that were not complete for every patient suggest that a more complete and larger assessment is necessary to draw a more definitive conclusion.

Genes 2024 , 11 Figure 2 .
Figure 2. The low resolution shows severe interstitial fibrosis with slightly less tubular atrophy, several globally sclerosed glomeruli, and moderate to severe intima fibrosis of an interlobular artery (blue arrow).In addition, a mild limpho-monocytic infiltration with frequent macrophages in scared areas and one tubular cyst (green arrow) could be observed.Trichrome, magnification ×400.

Figure 2 .
Figure 2. The low resolution shows severe interstitial fibrosis with slightly less tubular atrophy, several globally sclerosed glomeruli, and moderate to severe intima fibrosis of an interlobular artery (blue arrow).In addition, a mild limpho-monocytic infiltration with frequent macrophages in scared areas and one tubular cyst (green arrow) could be observed.Trichrome, magnification ×400.

Figure 3 .
Figure 3. Family trees (A-D).(A)The first family presented two brothers (generation II, subjects 1 and 3) affected by the DNAJB11 variant c.716 T>G (p.Leu239Ter), while their mother presented a non-diagnosed CKD.(B) In the second family, only the proband (generation II, subject 1) was diagnosed with the DNAJB11 variant c.134A>G (p.Tyr45Cys), while his siblings were not available for the family segregation.(C) In this third family, two cousins presented the DNAJB11 variant c.456+3_456+6del.Subject 2 of generation II also presented multicystic kidneys, although she never underwent genetic testing.Subject 3 of generation II did not show any signs or symptoms of CKD as she died at a young age.Finally, subject 1 of the generation I also presented CKD.(D) In the last family, subject 1 of generation II presented the DNAJB11 variant c.499C>T (p.Arg167Trp), her father presented CKD, but he was never evaluated with genetic testing.

Figure 3 .
Figure 3. Family trees (A-D).(A)The first family presented two brothers (generation II, subjects 1 and 3) affected by the DNAJB11 variant c.716 T>G (p.Leu239Ter), while their mother presented a non-diagnosed CKD.(B) In the second family, only the proband (generation II, subject 1) was diagnosed with the DNAJB11 variant c.134A>G (p.Tyr45Cys), while his siblings were not available for the family segregation.(C) In this third family, two cousins presented the DNAJB11 variant c.456+3_456+6del.Subject 2 of generation II also presented multicystic kidneys, although she never underwent genetic testing.Subject 3 of generation II did not show any signs or symptoms of CKD as she died at a young age.Finally, subject 1 of the generation I also presented CKD.(D) In the last family, subject 1 of generation II presented the DNAJB11 variant c.499C>T (p.Arg167Trp), her father presented CKD, but he was never evaluated with genetic testing.

Table 1 .
Summary of characteristics of the 5 patients described in the cohort from Bologna.In the DNAJB11 mutation column variants are expressed with their characteristics: HGVS classification; ACMG nomenclature; population frequency.N/A means Not Assessed.